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237891005: Autosomal recessive hypophosphatemic bone disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
356518014 Autosomal recessive hypophosphatemic bone disease en Synonym Active Entire term case insensitive SNOMED CT core module
356519018 Hypercalciuric rickets en Synonym Inactive Only initial character case insensitive SNOMED CT core module
356520012 HHRH - Hereditary hypophosphataemic rickets with hypercalciuria en Synonym Inactive Entire term case sensitive SNOMED CT core module
356521011 Autosomal recessive hypophosphataemic bone disease en Synonym Active Entire term case insensitive SNOMED CT core module
356522016 HHRH - Hereditary hypophosphatemic rickets with hypercalciuria en Synonym Inactive Entire term case sensitive SNOMED CT core module
626685017 Autosomal recessive hypophosphatemic bone disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive hypophosphatemic bone disease Is a Familial x-linked hypophosphatemic vitamin D refractory rickets false Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Finding site Cartilaginous tissue structure false Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Finding site Structure of osteoid tissue true Inferred relationship Existential restriction modifier 1
Autosomal recessive hypophosphatemic bone disease Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
Autosomal recessive hypophosphatemic bone disease Finding site Kidney structure false Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Autosomal recessive hypophosphatemic bone disease Occurrence Congenital false Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Is a Disorder with defective osteoid mineralization true Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Is a Hypophosphatemia true Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic bone disease Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive hypophosphatemic vitamin D refractory rickets Is a False Autosomal recessive hypophosphatemic bone disease Inferred relationship Existential restriction modifier
Autosomal recessive hypophosphatemic rickets Is a True Autosomal recessive hypophosphatemic bone disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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